ライフサイエンスコーパス: male

1 rocesses in the human brain (both female and male).

2 .2 (2.6) years; of the 115 included, 64 were male.

3 and 100 children, 51% (n = 51) of whom were male.

4 edian age was 78 years, and 73% (35/48) were male.

5 populations where females mate with multiple males.

6 ose associated diseases predominantly affect males.

7 GF2alpha in the porcine coronary artery from males.

8 menopausal females compared with age-matched males.

9 ed in accelerated liver tumor progression in males.

10 challenges from non-reproductive "bachelor" males.

11 es were bred with chow-fed sedentary C57BL/6 males.

12 ly prevalent, particularly among young adult males.

13 ssemblages in meerkat paste, particularly in males.

14 d LTL in females (all ps < 0.01), but not in males.

15 d food reinforcement was again found only in males.

16 cases and 58.32 [14.79] years for controls; male, 13 cases [46%] and 14 controls [50%]).

17 ng general surgery (101632 females and 72011 males), 130235 (75.0%) were categorized as elective, 225

18 Females (7124 [20.3%]) were less likely than males (13698 [24.4%]) to receive medications (P < .001),

19 quartile range {IQR}, 0.0-0.7%] of baseline; males: 3.4% [IQR, 0.4%-32.9%] of baseline; P < .001).

20 cruited 802 patients, of whom 360 (45%) were male, 442 (55%) were female; 158 (20%) were younger than

21 mized controlled trial, 128 young adults (71 male, 57 female) participated in 10 weeks of training wi

22 domized (mean [SD] age, 9.7 [5.3] years; 575 males [62%]), all completed the study.

23 Most of the dead were adult males (68%), but the highest case fatality (39%) was see

24 Median age was 43 years, 88% were black, 73% male, 69% had a history of injection drug use, 45% a his

25 Participants were 67% male, 84% non-Hispanic white, with mean age+/-SD 62+/-11

26 ignificantly higher graft failure risks than males (adjusted hazard ratios 0-14 years: 1.51 [95% conf

27 to quantify A1AR availability in 15 healthy male adults after 52 h of sleep deprivation and followin

28 reefrogs are able to select among individual males advertising for mates by taking advantage of small

29 ding the flight tones of multiple, tethered, male Ae. aegypti, we test the hypothesis that acoustic s

30 Twenty-one patients with BPES (10 female, 11 male) aged on average 15 years (range, 2-39 years), from

31 Twelve (92%) were male and 1 (8%) female, with an average age of 18.2 year

32 Twenty-two patients had XLP (9.7%; 10 male and 12 female patients), and 9 patients (4.0%) had

33 (2.8%) (mean [SD] age, 24.1 [6.1] years; 11 male and 16 female) presented with pathogenic or likely

34 (11)C-nicotine PET imaging of 11 healthy (5 male and 6 female) subjects.

35 Of the 100 observed patients, half were male and all were white; the mean (SD) age was 69.7 (14.

36 d 2(nd) instar larvae, mature larvae, pupae, male and female adults.

37 Young male and female Dmp1Cre.Socs3 (f/f) mice, in which SOCS3

38 en attributed to the differential effects of male and female gonadal secretions (commonly referred to

39 functional magnetic resonance imaging in 48 male and female healthy volunteers.

40 EEG was recorded while male and female human subjects watched and listened to v

41 tion of the levator auris longus muscle from male and female late-stage R6/2 mice and age-matched wil

42 measured visually evoked potentials in awake male and female mice before and after a 7 d monocular de

43 o investigate these differences, we infected male and female mice of different age groups with SARS-C

44 iking differences in gene expression between male and female mice, neither before nor after nerve inj

45 in DS, and that these phenotypes, present in male and female mice, provide novel means for examining

46 ic, and in vitro physiological techniques in male and female mice, we show that pulvinocortical termi

47 SCs) in the brain subependymal zone of adult male and female mice.

48 nction and breathing irregularities, in both male and female mice.

49 As male and female neurons in rodent BLA responded differen

50 sleep patterns, measured in advance in both male and female participants, predict subsequent pattern

51 lood gene expression response was similar in male and female patients.

52 ulated using OLINDA/EXM 1.2 for the standard male and female phantoms.

53 rotrophic assay and did not alter puberty in male and female rats or mammary gland development in fem

54 of the forebrain SBNN in juvenile and adult, male and female rats.

55 that ATZ has endocrine-disrupting effects on male and female reproduction in many vertebrate species.

56 ns SOHLH1 and SOHLH2 play important roles in male and female reproduction.

57 ictly regulated by factors derived from both male and female reproductive structures.

58 othalamic nucleus (VMH) mediating control of male and female sexual behavior, respectively.

59 the Glu(11) site to the Asp(1) site both in male and female transgenic mice in vivo and in cell line

60 Human participants (both male and female) were instructed to saccade toward a fac

61 Of 863 patients, 551 (63.9%) were male and median age was 58 years (interquartile range, 5

62 Two male and three female patients were recruited in this st

63 Human participants (21 males and 28 females) underwent an initial resting-state

64 performed on samples from 683 subjects (306 males and 377 females); 113 (16.5%) of 683 subjects were

65 Total 167 patients (95 males and 72 females) met the eligibility criteria and w

66 Y variants increase susceptibility to IAV in males and augment pathogenic immune responses in the lun

67 t preexposure increased fear conditioning in males and decreased generalization in females.

68 affect population dynamics requires tracking males and females (and sex-reversed individuals) separat

69 motion-related behaviors that differ between males and females and across the reproductive cycle.

70 ential radon with brain cancer mortality for males and females and the intensity of the correlation w

71 nd androgen receptors did not differ between males and females and were not sex-specifically altered

72 nsition was driven by mass migration of both males and females in roughly equal numbers, perhaps whol

73 early malnutrition and the implications for males and females respectively.

74 Sexually reproducing organisms require males and females to find each other.

75 of dystonia (LD) and healthy controls (both males and females), we identified an abnormally widespre

76 e allelic variants with different effects in males and females, and it has heterogeneous effects on t

77 d Spearman's Rho 0.509 (p-value < 0.001) for males and females, respectively.

78 ansgenic animals, including analysis of both males and females.

79 mately resulted in a doubling of fat mass in males and females.

80 ted schizophrenia-related phenotypes in both males and females.

81 at parental care can evolve independently in males and females.

82 ioural traits in our cohort differed between males and females; however Y chromosome and mitochondria

83 uccess in direct contest competition between males and in sexual coercion of females, thus increasing

84 hormone (GH) secretory profiles-pulsatile in males and persistent in females-regulate the sex-biased,

85 tivation in the PAG of females compared with males and was accompanied by increased transcription lev

86 These 'male' and 'female' model myocytes and tissues then were

87 asters athletes 54.4+/-8.5 years of age (70% male) and 92 controls of similar age, sex, and low Frami

88 Thirty-seven were male, and 43 were female.

89 After adjustment, patients who were older, male, and had atherosclerotic cardiovascular disease wer

90 Of the 575 patients with TOF, 57% were male, and the mean (SD) age was 31 (11) years.

91 ization had a mean age of 66 years, 73% were male, and the median baseline ankle-brachial index was 0

92 y higher proportions of drinkers were white, male, and with higher levels of education compared with

93 agement, genetic testing of African American males, and addressing the value framework of genetic eva

94 tic analogue of raspberry ketone (RK))-based male annihilation technique (MAT) are two of the most ef

95 the acute effects of cannabis on anxiety in males are mediated by the modulation of amygdalar functi

96 t cancer, although absolute excess risks for males are much less than for females.

97 es are ZZ, but in mammals females are XX and males are XY.

98 In birds, females are ZW and males are ZZ, but in mammals females are XX and males ar

99 re abundant and tightly packed in the NCM of males as compared to females.

100 ility and resilience studies have focused on males as one commonly used paradigm-chronic social defea

101 istic trait (spine length, a defence against males), as well as body size.

102 atural process of brain masculinization puts males at risk by moving them closer to a vulnerability t

103 oss-of-function mutations more frequently in males (based on a false discovery rate < 0.1), in compar

104 The male bias in the incidence of autism spectrum disorders

105 after treatment, gametocyte sex ratio became male-biased and was not significantly different between

106 er and secreted through the kidneys, exhibit male-biased expression.

107 ation in the cord blood of 39 females and 32 males born at term and with appropriate weight at birth

108 evels were all significantly higher in LG-IH male but not female offspring.

109 Male, but not female, deletion animals overexpress mRNA

110 Male, but not female, offspring of LPD mothers consisten

111 y fat, leptin, and insulin were increased in male, but not in female, F1 WD offspring.

112 Male C57BL/6 mice underwent 5/6 nephrectomy, and 8 weeks

113 le of ILK in hepatic insulin action in vivo, male C57BL/6J ILK(lox/lox) mice were crossed with Albcre

114 Six to eight week-old male C57BL/6J mice were fed with either a high-cholester

115 Male C57Bl6 mice ( 5 week old) were fed for 3 weeks prio

116 on distinct features of birdsong using adult male canaries (Serinus canaria), which show extensive se

117 have also investigated associations between male circumcision and risk of acquisition of HIV and sex

118 publications reporting associations between male circumcision and women's health outcomes up to Apri

119 y evidence was found for five outcomes, with male circumcision protecting against cervical cancer, ce

120 sh whether educating religious leaders about male circumcision would increase uptake in their village

121 of HIV-infected men resuming sex early after male circumcision.

122 urine samples and 46 saliva samples from 55 male college athletes ages 18-25 years.

123 Lifetime CVD risk was 64.8% for HIV-infected males compared to 54.8% for males in the US general popu

124 LV twist mechanics are reduced in males compared to females during reductions to adrenergi

125 activeness are more extended in bonobos [2], males compete less intensely for each mating opportunity

126 1 deficient ZZ fish grew much faster than ZZ male control.

127 d physical performance were worse than their male counterparts.

128 14 (P for trend <0.001), while mortality for males declined from 48.6% in 2002 to 32.2% in 2014 (P fo

129 eased difficulty of females finding mates as male density declines is the most frequently reported me

130 alleles become strongly associated with the male determining region, Y or Z).

131 ased organ donor, the PHS donor was younger, male, died from anoxia, more likely to be HCV and antibo

132 ng is a shared responsibility, but available male-directed contraceptive methods are either not easil

133 Male domestic short hair cats (n = 20), underwent either

134 se visible positions also displayed a strong male dominance over time that is eroding slowly.

135 ever-pregnant female donor, compared with a male donor, was associated with increased all-cause mort

136 Among recipients of male donors, females of all ages had significantly highe

137 These male DRD5KO mice also show reduced formalin pain respons

138 Never-smoker males drinking </=1 glass/week had significantly lower r

139 idence that flight tone interactions between males drive observed group coherence in the frequency do

140 presence of Ebola virus RNA in the semen of male Ebola survivors participating in the Postebogui stu

141 tis [UC], 234 with Crohn's disease [CD]; 236 male), enrolled in Germany from August 2013 through Apri

142 Conversely, in males, erasure leads to permanent X dosage decompensatio

143 ted with opponent categories (e.g., feminine male face).

144 We work an example involving data from male faces.

145 etween exposure to some pesticides and RA in male farmers.

146 oductive performance of resident and migrant males, females and pairs in a partially migratory bird.

147 of 1.5X faster rate of mutational decay of male fitness is nearly identical to the same ratio in Dr

148 object carrying serve to increase individual male fitness, yet are uncommon phenomena in the animal k

149 Daily treatment of adult male fmr1 C57Bl6 knock-out mice with BPN14770 for 14 day

150 confirming broad population-level impact in males from female HPV vaccination.

151 Male FVB/N-Tg(MMTVneu)202Mul/J (Her2) transgenic mice we

152 Furthermore, male Galapagos tortoises on Santa Cruz Island would be u

153 Rs to regulate gene expression in developing male gametes and histone retention in mature spermatozoa

154 Successful male gametogenesis involves orchestration of sequential

155 plays an important role in consolidating the male gametophytic ploidy consistency.

156 nivariate analysis, higher age (p = 0.0018), male gender (p = 0.019), high risk cytogenetics (p = 0.0

157 ired for embryonic development and regulates male germ cell development.

158 rtion (c.1297_8ins353, p.K433Rins31*) in the male germ cell-associated kinase (MAK) gene (39% of fami

159 d epigenetic features of closed chromatin in male germ cells, which suggests that CNVs may repress re

160 rols the mitosis-meiosis transition in mouse male germ cells.

161 The expression of DUO1 is restricted to the male germline and is first detected shortly after the as

162 and repetitive Y chromosomes in species with male heterogamety (XY), and W chromosomes in species wit

163 A representative sample of male high school students who graduated from high school

164 2 expansion was being driven by spinal onset males (HR 1.56 (95% CI 1.25 to 1.96).

165 econd, hermaphrodites recognize pheromone as male if the concentration of ascr#10 is higher than that

166 isolation-by-distance (IBD) than females and males in historic populations.

167 rphology and varied with the number of rival males in the pool, suggesting mechanisms selecting for c

168 for HIV-infected males compared to 54.8% for males in the US general population, but similar among fe

169 Although male individuals are three to four times more likely tha

170 could apply to treatment of disease such as male infertility.

171 cancer (PCa)-the most common cancer type in males-is completely unexplored.

172 In male Krt16(-/-) mice, oxidative stress associated with i

173 hybridization and RNAi assays indicate that males likely use biogenic amine neurotransmitters throug

174 enes already in an active chromatin state in male liver generally showed early cGH responses; genes i

175 ant, and ulcerated disease, especially among males living in the lowest SES neighborhoods.

176 cate that MC-IGC plasticity is induced after male-male social chemosensory encounters, resulting in e

177 102 hemispheres of in vivo MRI scans (N = 51 males, mean +/- SD 24.1 +/- 3.1 years of age) showed sim

178 and Cardiovascular Conditions) Registry (53% male; mean age 31 [range: 1-86 years]).

179 PENK in 1,908 patients with acute HF (1,186 male; mean age 75.66 +/- 11.74 years).

180 tive patients with lymphomas (45 females, 70 males; mean age of 46 years).

181 A total of 5626 patients (86.0% male; median [range] age, 58 [21-90] years) were identif

182 Of 111 patients included (67 [60%] male; median age, 75 [range, 24-94] years), 81 (73%) wer

183 population history, genealogy, forensics and male medical genetics.

184 in the somatic anther tissue is critical for male meiotic cell wall formation and thus plays an impor

185 Ptchd1 knock-out (KO) male mice exhibit cognitive alterations, including defec

186 or (ER) alpha compared with macrophages from male mice following allergen challenge.

187 The right knees of eight-week old male mice from two recombinant inbred lines (LGXSM-6 and

188 fat diet maintain CX3CL1-CX3CR1 levels while male mice show reductions in both ligand and receptor ex

189 ession of fluorescent marker into the VTA of male mice that had Cre-recombinase driven by OTR gene ex

190 C57BL/6 male mice were fed a Western diet (WD) +/-75 mg PDX twic

191 emyelination failure in the cuprizone model (male mice).

192 macrophages and neutrophils in the lungs of male mice, and depletion of inflammatory monocyte macrop

193 l, lysolecithin-demyelinated lesion in adult male mice.

194 lung and colon tissues from both female and male mice.

195 M2 gene promoters than did macrophages from male mice.

196 CAMK2G were altered in amygdala and mPFC of male mice.

197 on and cultural shift were instead driven by male migration, potentially connected to new technology

198 tage of these behavioural traits depended on male morphology and varied with the number of rival male

199 emale mortality was substantially lower than male mortality among the oldest-old, but that women's fu

200 strongly associated with higher working-age male mortality rates both between 1992 and 1998 (age-sta

201 Male moths compete to arrive first at a female releasing

202 scranial current stimulation of the rat (all males) motor cortex consisting of a continuous subthresh

203 archived rhesus macaque hippocampal samples (male, n = 13).

204 prevalence of sperm banking among adolescent males newly diagnosed with cancer and to identify factor

205 completed the study (56 +/- 8 years old; 62% male; nonalcoholic steatohepatitis etiology 24%; BMI 33.

206 oral corticosterone were investigated using male nonobese diabetic mice.

207 infection and, specifically, sexual minority males of color.

208 reased cardiovascular risk in mothers having male offspring suggests a maternal disease specific mech

209 olic expenditure and locomotor activities in male offspring, and increased number of pro-inflammatory

210 egnant rats causes reproductive disorders in male offspring, resulting from suppression of intratesti

211 l weight gain, were associated with NAFLD in male offspring.

212 Compared with male-only teams, female-only teams showed less hands-on

213 differences in wheel running or adiposity in male or female offspring, suggesting that changes in the

214 (45% fat) 4 weeks prior to mating with WT/KO males or heterozygous males with an ERalpha DNA-binding

215 ged >18 years, with waist circumference >94 (males) or >80 (females) cm, serum creatinine <1.2 mg/dL,

216 inductions of vitellogenin-like proteins in male organisms, inductions of Na(+)K(+)/ATPases, and str

217 r and showed slower bacterial clearance than males (P < 0.0001).

218 Female and male participants performed a modified location-cueing p

219 of 224 eyes (123 female participants and 101 male participants; mean [SD] age, 33.0 [15.1] years) had

220 By contrast, if female and male partners are both infected, embryos are viable.

221 .4%), black male patients (36.4%), and white male patients (30.2%, P<0.0001).

222 owed by white female patients (38.4%), black male patients (36.4%), and white male patients (30.2%, P

223 A total of 16 eyes of 5 female and 9 male patients were analyzed.

224 Male patients with XLP had significantly higher ePPIX le

225 Male pattern baldness (MPB) or androgenetic alopecia is

226 i acquired from 15 human participants (three males) performing a concurrent delayed match-to-sample t

227 iological models suggest that the biological male phenotype carries a higher intrinsic risk for ASD t

228 In this longitudinally monitored male population, observed effect of baseline central adi

229 were similar in men and women, with a slight male predominance.

230 Overall, male preponderance was seen except in the case of paroti

231 While the male preponderant prevalence of ASD might partially be e

232 CASE REPORT: A 50-year-old male presented with acute urinary retention.

233 remission and abstinence over 3 months among male primary care attendees with harmful drinking in a s

234 Adult male rainbow darter (RBD) (Etheostoma caeruleum) were co

235 ecorded in anesthetized and ventilated adult male rats and a multielectrode array was used to record

236 Male rats learned to associate one context with sucrose

237 across all vigilance states in freely moving male rats to determine whether the RSC and the ACA are e

238 ut not maintenance, of morphine tolerance in male rats.

239 ted with increased all-cause mortality among male recipients but not among female recipients.

240 As such, PFOS-induced male reproductive dysfunction can possibly be managed th

241 ity to the liver, the immune, endocrine, and male reproductive systems, and the developing fetus and

242 tial means to reduce ZIKV persistence in the male reproductive tract.

243 model to study RNA virus persistence in the male reproductive tract.

244 Here, we show that male rhesus macaques can learn categories by a transitiv

245 Bigger males scheduled earlier routines that aligned more close

246 netic stimulation of oxytocin neurons render males sensitive to the distress of an unfamiliar mouse.

247 ring system consisted of clinical variables (male sex and previous percutaneous coronary intervention

248 iological and disease processes sensitive to male sex hormone actions, thereby not only affecting the

249 Female to male sex reversal was achieved in an emerging agricultur

250 ypically leads to masculinization (female-to-male sex reversal), resulting in neomales.

251 asthma who consented, 286 (mean age, 7.7 yr; male sex, 65.8%) were mite sensitized, and 284 were rand

252 associated with nonwhite race, younger age, male sex, and lack of access to health care.

253 high-intensity statin prescriptions included male sex, filling beta-blocker and antiplatelet agent pr

254 was associated with older age at diagnosis, male sex, poor initial levodopa treatment response, and

255 nts considered "too well" were advanced age, male sex, university hospital admission, comorbidity, an

256 th higher intelligence, East Asian ancestry, male sex, younger age, formal music training-especially

257 nd when MS1 neurons are silenced, the normal male sleep suppression in female presence is attenuated

258 When MS1 neurons are activated, isolated males sleep less, and when MS1 neurons are silenced, the

259 Dmrt1 exhibited early male-specific embryonic expression, preceding the onset

260 es, compensation involves recruitment of the male-specific lethal (MSL) complex to X-linked genes and

261 ion, the CLAMP (chromatin-linked adaptor for male-specific lethal [MSL] proteins) zinc finger protein

262 ereby not only affecting the pathogenesis of male-specific prostate cancer but also likely contributi

263 operties of the human Y chromosome - namely, male specificity, haploidy and escape from crossing over

264 the institutional animal care committee, 60 male Sprague-Dawley rats were fed either a standard chow

265 Four male Sprague-Dawley rats with different blood glucose co

266 ts auditory processing in large areas of the male starling brain.

267 We report here the cloning of Male Sterile23 (Ms23), encoding an anther-specific predi

268 ng of the Ms2 gene and show that Ms2 confers male sterility in wheat, barley and Brachypodium.

269 KEY MESSAGE: We have developed a unique male-sterility and fertility-restoration system in rice

270 Healthy male subjects (n=29) participated in two randomized trea

271 ationships among HCV sequences from the four male subjects and subsequent transmission from one subje

272 e enrolled a convenience sample of 220 adult male survivors of EVD in Sierra Leone, at various times

273 sses were detected in the blubber of 4 adult male T. truncatus.

274 igher radiation-associated relative risk for male than for female breast cancer, although absolute ex

275 with the higher rates of ASD observed among males than among females in the general population.

276 ous aortic dissection tended to be higher in males than females (25% versus 18%, P=0.06); 44% of diss

277 er (ASD) is known to be more prevalent among males than females in the general population.

278 y be more sensitive to adrenergic control in males than in females.

279 Males that call from very shallow water bodies (few mm d

280 tis (mean [SD] age, 62.3 [18.9] years; 59.1% male), the standardized annual incidence was stable betw

281 Compared with the proximal tubule of males, the proximal tubule of females had greater phosph

282 re associated with direct benefits, enabling males to maximize offspring production.

283 cate that females may be more sensitive than males to stress-induced drug seeking.

284 deletion of this entire region results in a male-to-female conversion, whereas loss of a single supp

285 ngle suppressor of female development drives male-to-hermaphrodite conversion.

286 ot (age >/=16 y; mean age, 35.8+/-10.1 y; 38 male) undergoing PVR were prospectively recruited for ca

287 pathogenic role of Mycoplasma genitalium in male urethritis is clear, fewer studies have been conduc

288 rs (MOR) of 22 healthy recreationally active males using positron emission tomography (PET) and the M

289 ed in testicular and sperm function in adult males via interaction with relaxin/insulin-like family p

290 In males, WAY100635/GR127935 was most effective in reducing

291 hile specificity and NPV of MALDI-TOF MS for males were significantly higher than those for females (

292 305 patients (mean age 73 +/- 11 years; 75% male) were included.

293 t fish with undifferentiated gonads were all males, who grew larger than the genetic females during t

294 mediated via actions on local OXT neurons in male Wistar rats.

295 We analysed data from 14 adult males with adult cerebral adrenoleukodystrophy treated w

296 r to mating with WT/KO males or heterozygous males with an ERalpha DNA-binding domain mutation knocke

297 "Leader" males with harems putatively use loud calls to deter cha

298 dults (median age at entry 22.6 years, 50.6% males) with CHD (49% simple, 39% moderate, and 12% compl

299 e most common macular degenerations in young males, with a worldwide prevalence ranging from 1:5000 t

300 eas Xa contained abundant mCH similar to the male X chromosome and the autosomes.